ENST00000295897.9:c.1182T>C
MANE Select
|
ENSP00000295897.4:p.Tyr394=
|
|
ENST00000295897.8:c.1182T>C
|
ENSP00000295897.4:p.Tyr394=
|
|
ENST00000401494.7:c.837T>C
|
ENSP00000384695.3:p.Tyr279=
|
|
ENST00000415165.6:c.606T>C
|
ENSP00000401820.2:p.Tyr202=
|
|
ENST00000476441.6:c.*461T>C
|
ENSP00000423727.1:n.*461T>C
|
|
ENST00000484992.1:n.502T>C
|
|
|
ENST00000503124.5:c.732T>C
|
ENSP00000421027.1:p.Tyr244=
|
|
ENST00000504043.1:n.185T>C
|
|
|
ENST00000505649.5:n.868T>C
|
|
|
ENST00000509063.5:c.1182T>C
|
ENSP00000422784.1:p.Tyr394=
|
|
ENST00000511370.1:c.715T>C
|
|
|
ENST00000621085.4:c.543T>C
|
ENSP00000483421.1:p.Tyr181=
|
|
ENST00000621628.4:c.543T>C
|
ENSP00000480485.1:p.Tyr181=
|
|
NM_000477.5:c.1182T>C
|
NP_000468.1:p.Tyr394=
|
|
NM_000477.6:c.1182T>C
|
NP_000468.1:p.Tyr394=
|
|
NM_000477.7:c.1182T>C
MANE Select
|
NP_000468.1:p.Tyr394=
|
|